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You searched for: Author/Creator Van Mossevelde, Sara

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1. [P4–069]: A PROSPECTIVE NEUROGENETIC STUDY ON EARLY‐ONSET DEMENTIA IN PATIENTS WITH UNCLEAR INITIAL DIAGNOSIS OF DEGENERATIVE DEMENTIA. (1st July 2017)

3. [P4–075]: THE MAPT P.ARG406TRP IS A FOUNDER MUTATION IN BELGIUM AND PRESENTS WITH AN ALZHEIMER DISEASE DEMENTIA‐LIKE PHENOTYPE. (1st July 2017)

4. DT‐02‐01: Loss‐of‐function mutations in TBK1 are frequently associated with frontotemporal lobar degeneration in a belgian patient cohort. (1st July 2015)

5. Extensive genetic and phenotypic description of MAPT p.R406W in the Flanders‐Belgian population. (1st February 2022)

6. Extensive genetic and phenotypic description of MAPT p.R406W in the Flanders‐Belgian population. (December 2021)

7. In‐depth phenotypic description of pathogenic TBK1 mutations: A frequent cause of FTD and ALS in the Flanders‐Belgian population. (1st February 2022)

8. In‐depth phenotypic description of pathogenic TBK1 mutations: A frequent cause of FTD and ALS in the Flanders‐Belgian population. (December 2021)

9. Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohort. (15th December 2015)

10. Microtubule associated protein tau p.R406W patient carriers present with a nonconforming clinical phenotype. (20th December 2022)